1. Academic Validation
  2. Isoquinolines from the roots of Thalictrum flavum L. and their evaluation as antiparasitic compounds

Isoquinolines from the roots of Thalictrum flavum L. and their evaluation as antiparasitic compounds

  • Molecules. 2010 Sep 16;15(9):6476-84. doi: 10.3390/molecules15096476.
Jacqueline Ropivia 1 Séverine Derbré Caroline Rouger Fabrice Pagniez Patrice Le Pape Pascal Richomme
Affiliations

Affiliation

  • 1 Laboratoire des Substances d'Origine Naturelle et Analogues Structuraux, UPRES-EA 921, IFR 149 QUASAV, UFR des Sciences pharmaceutiques et ingénierie de la santé, Université d'Angers, Angers, France.
Abstract

Alkaloids from Thalictrum flavum L. (Ranuculaceae) growing in the Loire valley (France) were isolated and evaluated for their antiplasmodial and leishmanicidal activities. Berberine was identified as a major component but its analogue, pseudoberberine, was isolated for the first time from this plant. As far as bisbenzylisoquinolines are concerned, thalfoetidine was also isolated and, besides, its nor- derivative, northalfoetidine, was identified as a new compound. Previously isolated Alkaloids from Thalictrum species such as northalidasine, northalrugosidine, thaligosidine, thalicberine, thaliglucinone, preocoteine, O-methylcassythine and armepavine were newly described in the roots of T. flavum. Tertiary isoquinolines, and particularly bisbenzylisoquinolines, were found to be leishmanicidal against L. major. Thalfoetidine appeared as the most potent but its new nor- derivative northalfoetidine, as well as northalidasine, were of particular interest due to the fact that their potential leishmanicidal activity was not associated to a strong cytotoxicity.

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